Allopurinol

Generic: allopurinol

Labeler: Preferred Pharmaceuticals Inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Active

Drug Facts

Product Profile

Brand Name Allopurinol
Generic Name allopurinol
Labeler Preferred Pharmaceuticals Inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ALLOPURINOL 100 mg/1

Identifiers & Regulatory

Product NDC 68788-7383
Product ID 68788-7383_69dddabb-8066-4162-9260-554a2c764116
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203154
Listing Expiration 2026-12-31
Marketing Start 2016-09-13

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687887383
Hyphenated Format 68788-7383

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name Allopurinol (source: ndc)
Generic Name allopurinol (source: ndc)
Application Number ANDA203154 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68788-7383-3)
  • 60 TABLET in 1 BOTTLE (68788-7383-6)
  • 90 TABLET in 1 BOTTLE (68788-7383-9)
source: ndc

Packages (3)

68788-7383-3 30 TABLET in 1 BOTTLE (68788-7383-3) 68788-7383-6 60 TABLET in 1 BOTTLE (68788-7383-6) 68788-7383-9 90 TABLET in 1 BOTTLE (68788-7383-9)

Ingredients (1)

ALLOPURINOL (100 mg/1)

Linked Drug Pages (1)

Allopurinol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "69dddabb-8066-4162-9260-554a2c764116", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319"], "spl_set_id": ["62866c84-fec3-4c1b-9b8b-65c0372bc8f9"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7383-3)", "package_ndc": "68788-7383-3", "marketing_start_date": "20160913"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-7383-6)", "package_ndc": "68788-7383-6", "marketing_start_date": "20160913"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7383-9)", "package_ndc": "68788-7383-9", "marketing_start_date": "20160913"}], "brand_name": "Allopurinol", "product_id": "68788-7383_69dddabb-8066-4162-9260-554a2c764116", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "68788-7383", "generic_name": "allopurinol", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "ANDA203154", "marketing_category": "ANDA", "marketing_start_date": "20160913", "listing_expiration_date": "20261231"}